Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Qigong program for managing pain in people with spinal cord injuries

Official title: HAPPINESS: cHAnging the Perceived Pain INtEnSity in Populations With Spinal Cord Injury and With Health Disparities: A Feasibility Study

Run by University of Minnesota · NCT06140355 · Data updated 2026-11-12

This study is testing a 12-week online Qigong program to see if it can help adults with spinal cord injuries manage their chronic pain better.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorUniversity of Minnesota
Academic / other
Locations3 sites (Miami, Florida and 2 other locations)
StatusRecruiting
StartedAugust 20, 2024
Main results expectedJanuary 31, 2027
Study endsJanuary 31, 2027
Registry record updatedAugust 19, 2026
Trial IDNCT06140355 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 and older with spinal cord injuries experiencing neuropathic pain rated 4 or above on a pain scale.

Probably not a fit

Patients with uncontrolled seizure disorders, cognitive impairments, or those currently practicing Tai Chi or Qigong regularly may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the feasibility of a 12-week remote Qigong program aimed at reducing chronic neuropathic pain in adults with spinal cord injuries. Participants engage in Qigong practices through online videos, with the goal of improving their pain management. The study previously showed promising results, with significant pain reduction observed after the intervention and sustained benefits at follow-up. The program is designed to be accessible for individuals with spinal cord injuries, requiring only internet access and basic technology.

Why it matters

Potential benefit: If successful, this program could provide a non-pharmacological approach to significantly reduce pain for individuals with spinal cord injuries.

How similar studies have gone: Previous studies have shown positive outcomes with Qigong for pain management, indicating potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 18+ years old
* medically stable
* with neuropathic pain 4 or above on the numeric pain rating scale + screened with painDETECT
* willing to participate in a remote Qigong intervention (from any location with internet connection)
* fluent in English or Spanish
* access to the internet and a computer/iPad or smartphone

Exclusion Criteria:

* uncontrolled seizure disorder
* cognitive impairment and/or communicative disability (e.g., due to brain injury) preventing them from following directions or from learning
* ventilator dependency
* major medical complications
* pressure ulcers hindering prolonged sitting or lying down
* (planning to become) pregnant or planning a major surgery during the study (given study duration, regular Qigong practice, and frequent check-ins)
* regular Tai Chi or Qigong practice in the past 6 months (3x/week or more)
* currently engaged in other rehabilitation programs that would influence outcomes

Where it's running

  • University of Minnesota
    Minneapolis, Minnesota, United States
    Recruiting
  • University of Miami
    Miami, Florida, United States
    Not yet recruiting
  • University of Texas - Rio Grande Valley
    Harlingen, Texas, United States
    Not yet recruiting

Study contacts

  • Principal investigator: Ann Van de Winckel, PhD, MSPT, PT — University of Minnesota
  • Study coordinator: Ann Van de Winckel, PhD, MSPT, PT
  • Email: avandewi@umn.edu
  • Phone: 612-625-1191

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.